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CCXXXVII.—The preparation of phthalamic acids and their conversion into anthranilic acids. Ernest Chapman, Henry Stephen , J. Chem. Soc., Trans. , 1925 , 127 , 1791

Impact of planarity of unfused aromatic molecules on G-quadruplex binding: Learning from isaindigotone derivatives. Jin-Qiang Hou, Jia-Heng Tan, Xiao-Xiao Wang, Shuo-Bin Chen, Si-Yuan Huang, Jin-Wu Yan, Shu-Han Chen, Tian-Miao Ou, Hai-Bin Luo, Ding Li, Lian-Quan Gu, Zhi-Shu Huang , Org. Biomol. Chem. , 2011 , 9 , 6422

162. Xanthones and thioxanthones. Part I. The synthesis of 2- and 3-dialkylaminoalkylamino-derivatives. Frederick G. Mann, J. Hedley Turnbull , J. Chem. Soc. , 1951 , 747

Facile and versatile access to substituted hexabenzoovalene derivatives: characterization and optoelectronic properties. Lijiao Wang, Wei Hao, Yanbing Han, Yamei Shi, Shuzhou Li, Chunfang Zhang, Jinchong Xiao , Org. Biomol. Chem. , 2019 , 17 , 7964

Chimerically designed HDAC- and tyrosine kinase inhibitors. A series of erlotinib hybrids as dual-selective inhibitors of EGFR, HER2 and histone deacetylases. Thomas Beckers, Siavosh Mahboobi, Andreas Sellmer, Matthias Winkler, Emerich Eichhorn, Herwig Pongratz, Thomas Maier, Thomas Ciossek, Thomas Baer, Gerhard Kelter, Heinz-Herbert Fiebig, Mathias Schmidt , Med. Chem. Commun. , 2012 , 3 , 829

88. The chemistry of simple heterocyclic systems. Part I. Reactions of 6- and 7-nitro-4-hydroxyquinazoline and their derivatives. J. S. Morley, J. C. E. Simpson , J. Chem. Soc. , 1948 , 360

CCCXXXIII.—Tetrahydroacridine, octahydroacridine, and their derivatives. William Henry Perkin, William Greenwell Sedgwick , J. Chem. Soc., Trans. , 1924 , 125 , 2437

356. Synthetic antimalarials. Part XXXI. 2-p-chloroanilino-4-β-diethylaminoethylaminoquinazolines containing various substituents in the quinazoline nucleus. F. H. S. Curd, J. K. Landquist, F. L. Rose , J. Chem. Soc. , 1948 , 1759

768. Nitration of 2-acetamido-5-methoxytoluene. J. MacMillan , J. Chem. Soc. , 1952 , 4019

Substituent effects on the kinetics of reductively-initiated fragmentation of nitrobenzyl carbamates designed as triggers for bioreductive prodrugs. Michael P. Hay, Bridget M. Sykes, William A. Denny, Charmian J. O’Connor , J. Chem. Soc., Perkin Trans. 1 , 1999 , 2759